Evidence map›Paper›PMID 32847908›Full record

Observational studyBMJ open2020

On the path towards universal coverage of hepatitis C treatment among people receiving opioid agonist therapy (OAT) in Norway: a prospective cohort study from 2013 to 2017.

Christer Frode Aas, Jørn Henrik Vold, Svetlana Skurtveit, Ingvild Odsbu, Fatemeh Chalabianloo, Jan Magnus Økland, Rafael Alexander Modahl Leiva, Peter Vickerman, Kjell Arne Johansson, Lars T Fadnes

Abstract readObservational Study
In one paragraph

Observational study in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Christer Frode AasDepartment of Addiction Medicine, Helse Bergen HF, Bergen, Norway christer.frode.aas@helse-bergen.no.ORCID 0000-0002-6469-9354
Jørn Henrik VoldDepartment of Addiction Medicine, Helse Bergen HF, Bergen, Norway.
Svetlana SkurtveitDepartment of Mental Disorders, Norwegian Institute of Public Health, Oslo, Norway.
Ingvild OdsbuDepartment of Medicine, Karolinska Institute, Stockholm, Sweden.
Fatemeh ChalabianlooDepartment of Addiction Medicine, Helse Bergen HF, Bergen, Norway.
Jan Magnus ØklandDepartment of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Rafael Alexander Modahl LeivaDepartment of Infectious Diseases, Helse Bergen, Bergen, Norway.
Peter VickermanLondon School of Hygiene and Tropical Medicine, London, UK.
Kjell Arne JohanssonDepartment of Addiction Medicine, Helse Bergen HF, Bergen, Norway.
Lars T FadnesDepartment of Addiction Medicine, Helse Bergen HF, Bergen, Norway.ORCID 0000-0001-8757-2092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed to calculate cumulative hepatitis C virus (HCV) treatment coverage among individuals enrolled in opioid agonist therapy (OAT) in Norway between 2013 and 2017 and to document the treatment transition to direct-acting antiviral (DAA) agents. Moreover, we aimed to describe adherence to DAAs in the same cohort.

designProspective cohort, registry data.

settingSpecialist healthcare service (secondary) PARTICIPANTS AND OUTCOMES: This observational study was based on data from The Norwegian Prescription Database. We studied dispensed OAT and HCV treatment annually to calculate the cumulative frequency, and employed secondary sources to calculate prevalence, incidence and HCV treatment coverage from 2013 to 2017, among the OAT population. Factors associated with adherence to DAAs were identified a priori and subject to logistic regression.

results10 371 individuals were identified with dispensed OAT, 1475 individuals of these were identified with dispensed HCV treatment. Annual HCV treatment coverage increased from 3.5% (95% CI: 3.2 to 4.4) in 2013 to 17% (95% CI: 17 to 20) in 2017, giving a cumulative HCV coverage among OAT patients in Norway of 38.5%. A complete shift to interferon-free treatment regimens occurred, where DAAs accounting for 32% of HCV treatments in 2013 and 99% in 2017. About two-thirds of OAT patients were considered adherent to their DAA regimens across all genotypes. High level of OAT continuity was associated with improved adherence to DAAs (adjusted OR 1.4, 95% CI: 1 to 2, p=0.035).

conclusionsA large increase in HCV treatment coverage attributed by a complete shift to interferon-free regimens among the Norwegian OAT population has been demonstrated. However, treatment coverage is inadmissibly too low and a further substantial scale-up in HCV treatment is required to reach the universal targets of controlling and eliminating the HCV endemic.

Indexed as

Hepatitis CHepatitis C, ChronicAnalgesics, OpioidAntiviral AgentsCohort StudiesHumansNorwayProspective StudiesUniversal Health InsuranceAnalgesics, OpioidAntiviral Agentsepidemiologyhealth policyinfection controlinfectious diseasesorganisation of health servicessubstance misuse

Identifiers

PMID32847908
PMCPMC7451452

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.